HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 4-[(R)-3-(3,5-Dichloro-4'-methoxycarbonyl-biphenyl-4-ylmethyl)-2-oxo-pyrrolidin-1-yl]-piperidine-1-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methoxycarbonylphenylboronic acid | HCID 2734369 | — |
| Reactant | 4-[3-(2,6-Dichloro-4-trifluoromethanesulfonyloxy-benzyl)-2-oxo-pyrrolidin-1-yl]-piperidine-1-carboxylic acid tert-butyl ester | HCID 86629121 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-[(R)-3-(3,5-Dichloro-4'-methoxycarbonyl-biphenyl-4-ylmethyl)-2-oxo-pyrrolidin-1-yl]-piperidine-1-carboxylic acid tert-butyl ester | HCID 66671551 | 88% |
Reaction Steps
Treat a solution of 4-[3-(2,6-Dichloro-4-trifluoromethanesulfonyloxy-benzyl)-2-oxo-pyrrolidin-1-yl]-piperidine-1-carboxylic acid tert-butyl ester (Preparation 15) (0.5 g, 0.9 mmol), 4-methoxycarbonylphenylboronic acid (0.31 g, 1.7 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.1 g, 0.1 mmol) in DME (5 mL) with 2M aqueous K2CO3 (1.3 mL), heat the reaction to 80° C., and stir overnight. Cool the reaction and quench with 1N HCl. Extract the aqueous with EtOAc. Wash the organic with brine, dry over MgSO4, and filter. Purify the crude by silica gel column chromatography using Hexanes:EtOAc to elute the pure product. Remove the solvent to afford 0.43 g (88%) of desired product. MS (m/e): 583 (M+Na+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07829582B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-2284cfd9b20f424b95485fc93d29f6fe |
| Source note | uspto-grants-2010_11 |